HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234496Generated: October 31, 2026
Diisopropylethylamine → 4-amino-2,5-difluoro-N-[(3R)-1-methylpyrrolidin-3-yl]benzamide
https://huagongshe.com/reaction/2234496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Amino-2,5-difluorobenzoic acid | HCID 20151477 | — |
| Reactant | (3R)-1-Methyl-3-PyrrolidinaMine hydrochloride | HCID 53256048 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-amino-2,5-difluoro-N-[(3R)-1-methylpyrrolidin-3-yl]benzamide | HCID 68682472 | — |
Reaction Steps
4-amino-2,5-difluoro-benzoic acid (Rare Chemicals GmbH; 450 mg, 2.6 mmol), (3R)-1-methylpyrrolidin-3-amine di Hydrochloride (Intermediate 184; 473 mg, 2.73 mmol), HATU (1.08 g 2.86 mmol) and DIPEA (2.25 mL, 13 mmol) were combined in DMF (10 mL) and stirred at room temperature for 4 hours. The solvent was evaporated and the residue dissolved in MeOH and added to an SCX-2 column (20 g), pre-wet with MeOH (2 column volumes). The column was flushed with MeOH (2 column volumes) and eluted with 2M ammonia in MeOH. Product containing fractions were combined and evaporated and the resultant material dissolved in DCM and purified on a silica column eluting with 5% 2M ammonia in MeOH/DCM. Fractions containing product were combined and evaporated to a yellow gum. Diethylether was added and re-evaporated and dried under high vacuum to yield the title compound as a yellow gum, which slowly crystallised to a cream solid (550 mg, 83%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07709471B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-328318b4be35479781975f95c2c99831 |
|---|
| Source note | uspto-grants-2010_05 |
|---|